Терапевтический архив (Sep 2020)

Multipotent mesenchymal stromal cells application for acute graft versus host disease treatment

  • L. A. Kuzmina,
  • N. A. Petinati,
  • V. A. Vasilieva,
  • M. V. Dovydenko,
  • M. Yu. Drokov,
  • Yu. O. Davydova,
  • N. M. Kapranov,
  • N. V. Sats,
  • Yu. A. Chabaeva,
  • S. M. Kulikov,
  • T. V. Gaponova,
  • N. I. Drize,
  • E. N. Parovichnikova,
  • V. G. Savchenko

DOI
https://doi.org/10.26442/00403660.2020.07.000757
Journal volume & issue
Vol. 92, no. 7
pp. 23 – 30

Abstract

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Aim.Analysis of the effectiveness of the MSCs aministration as the second- or third-line therapy of acute GVHD (aGVHD) resistant to glucocorticosteroid treatment. Materials and methods.The study included 35 patients who received MSCs obtained from the bone marrow of healthy donors as a treatment of steroid-resistant aGVHD. The clinical parameters of patients, MSCs cultural characteristics, the MSC expression profile for various genes including those involved in immunomodulation, expression of cells surface markers, the source of MSCs, as well as the frequency and number of MSC administrations were analyzed. Results.Response to therapy was achieved in 74% of cases, a complete response was reached in 13 (37%) patients, partial response/clinical improvement was demonstrated in 13 (37%). This treatment was ineffective in 9 patients. The prediction of a group of patients with good response to MSC therapy turned to be impossible. The differences between the effective and ineffective for the GVHD treatment MSCs samples were found. The effective ones were characterized with a decreased total MSCs production and an increase in the main histocompatibility complex and PDL-1 antigens expression. Conclusion.These data allow to select optimal samples for aGVHD treatment that can improve clinical results. aGVHD treatment with MSCs has shown efficacy comparable to other treatment approaches. Given the low percentage of complications and the absence of significant adverse effects, MSC therapy seems to be one of the optimal approaches to the treatment of resistant forms of GVHD.

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